ryze - Version CMR - Clinical Metadata Repository Software
ryze clinical metadata repository is the easiest way to manage & reuse standards and studies. Imagine if all your study content – standards, forms, datasets, mappings… were in 1 place. And they were all interconnected. Everything from eCRFs to submission deliverables. No matter where they were, your teams could manage standards and studies, share and reuse content – even across different EDCs and e-clinical systems. That’s ryze. The all-in-1 fully integrated clinical metadata repository. And you can start now. It’s ready out-the-box – no long and complex implementation.
Creating clinical study builds from scratch is far quicker and easier with our clinical metadata management software. You’ve got pre-approved, consistent content in your clinical metadata repository. And this can be reused forevermore across your studies and standards. Instead of starting out with nothing, you’ve got an entire library of content ready to go!
Because your content is in 1 place, you don’t need to go hunting for it. Everything held in your studies and standards is right there for all to see. Different teams can get at the metadata they need, and easily share and approve content. Plus, you save acres of time reusing study metadata. There’s no need to retype file contents every single time!
Increase the quality of studies by reusing content from your standards library in our clinical metadata repository. You’re not constantly retyping stuff, so there’s no manual errors. And because you’re using standardized content, you know it’s already been approved internally.
By managing standards and building study libraries in ryze, you really cut study build costs. You get started so much faster because most of your content is already there in your clinical metadata repository. And if the data you want isn’t there, just import it into your ryze library from your EDC, e-clinical or internal systems!
The ryze MDR platform incorporates a clinical metadata repository (MDR), or a cloud MDR! Think of it as a central library where all your clinical metadata is held and managed. All of your content is connected, from eCRFs through to submission deliverables. You can easily find, review, reuse, and share content – including across different EDC and other external systems.
1 home for your metadata
Different departments can access studies and organizational standards in one place for your MDR clinical trials. You can assign work to specific individuals, and allow parallel review by multiple specified users. This gives greater transparency and enables better communication amongst your team. Global search functionality makes it quick and easy to find studies, standards, and assets in your clinical metadata repository.
Easily manage changes
With ryze MDR automation platform, you can easily manage changes and consider impacts. You benefit from a structured process that adheres to regulatory compliance. And this, in turn, reduces associated risk. Find out more about change management in ryze.
How our metadata management tools make things easier
You can create and manage your organizational standards in your clinical metadata repository. This includes importing content from your EDC, e-clinical database, or other external systems. This helps to increase your data quality and decreases downstream costs. By creating consistent forms and datasets, building studies from scratch is now quick and easy!
For studies and standards, you can include any related links. For example, you can link to a CDISC Therapeutic Area User Guide with instructions for how to use a CRF or dataset. You can also add any related files, such as the protocol or statistical analysis plan.
With all your content in 1 place, it’s easy to find what you’re looking for. Rather than wasting time trying to find content or rely on others for it, quickly search across all your standards and studies in the ryze MDR automation platform – get the content you need, super-fast.
Easily update and improve your organizational standards in ryze over time. Because of in-built quality processes, you can be sure that you’re always using the correct version of a standard. You can therefore improve consistency and data quality across studies.
There’s full traceability in the ryze cloud MDR. You can see a full and detailed lifecycle history of a standard. You can also see where a standard is used in studies. Plus any changes made to that standard over time. Compare a study to your standards, or other studies. Detailed difference reports instantly show the changes. That way you have complete visibility and transparency between team members.
Reuse content in your clinical metadata repository across standards and studies. You can easily import standardized content from your EDC or e-clinical database. In other words, import forms, datasets, mappings, edit checks, mappings etc into ryze to store and reuse. This saves lots of time because there’s no retyping. And because you’re using pre-approved content, you know it’s correct.
You’re in control. You decide what lifecycle stages you want in your standards and studies. It all depends on what makes sense for your company. Alternatively, just use the default lifecycle in ryze that’s ready to use.
Our API lets your system automatically communicate with our ryze clinical metadata repository. No logging into the ryze platform and manually uploading or downloading data. Instead, you can have a direct link to automatically see study metadata. This saves time and means you can set up automatic processes, for example, to synchronize data.